Hps. Makkar et al., NUTRIENT CONTENTS, RUMEN PROTEIN DEGRADABILITY AND ANTINUTRITIONAL FACTORS IN SOME COLOR-FLOWERING AND WHITE-FLOWERING CULTIVARS OF VICIA-FABA BEANS, Journal of the Science of Food and Agriculture, 75(4), 1997, pp. 511-520
Six colour-flowering (Scirocco, Alfred, Carola, Condor, Tina and Herz
Freya) and six white-flowering (Caspar, Albatros, Gloria, Tyrol, Vasco
and Cresta) cultivars of Vicia faba were studied. The crude protein c
ontents of colour-and white-flowering cultivars were 267 +/- 13.6 and
283 +/- 18.8 g kg(-1), respectively, which did not differ significantl
y at P < 0.05. The levels of lipids, crude fibre, starch and ash varie
d from 14 to 22 g kg(-1), 88 to 143 g kg(-1), 407 to 485 g kg(-1) and
32 to 42 g kg(-1), respectively. The calculated organic matter digesti
bility (OMD) and metabolisable energy (ME) of the white-flowering cult
ivars were significantly higher (P < 0.001) than those of the colour-f
lowering cultivars (OMD: 889.1 +/- 26.6 g kg(-1) vs 797.5 +/- 17.1 g k
g(-1); ME: 13.97 +/- 0.49 vs 12.30 +/- 0.34 MJ kg(-1)). In all cultiva
rs, sulphur amino acids were lower than adequate concentration when co
mpared with recommended amino acid pattern of FAG/WHO/UNO reference pr
otein for a 2-5-year-old child. The in vitro rumen nitrogen degradabil
ity of colour-flowering cultivars was significantly lower (P < 0.01) c
ompared to that of white-flowering cultivars (71.4 +/- 9.3% vs 88.0 +/
- 11.1%). Amongst colour-flowering varieties, the contents of total ph
enols (TP), tannins (T) and condensed tannins (CT) were highest in Alf
red (28.3, 21.0 and 35.4 g kg(-1), respectively). The contents of TP a
nd T were similar (about 15 and 10 g kg(-1), respectively) in Carola,
Tina and Herz Freya, and the CT were in the order: Condor > Herz Freya
> Carola. The CT were not detected in white-flowering varieties, T we
re virtually absent and TP were extremely low (4.0-4.9 g kg(-1)). The
activities of other antinutritional factors (white- and colour-floweri
ng cultivars, respectively: trypsin inhibitor activity 3.05 +/- 0.34 a
nd 1.85 +/- 0.09 mg trypsin inhibited g(-1); lectin 27.2 +/- 9.4 and 2
7.1 +/- 5.1 mg ml(-1) assay medium producing haemagglutination; phytat
e 15.0 +/- 2.7 and 16.6 +/- 2.3 g kg(-1)) were very low. A strong nega
tive correlation (r = -0.92, P < 0.001) between tannins and in vitro r
umen protein degradability was observed which suggested that tannins h
ave adverse effect on protein degradability. Similarly negative correl
ations between tannin levels and metabolisable energy (r = -0.89; P <
0.001) and organic matter digestibility (r = -0.89; P < 0.001) were ob
served. The correlation coefficient between trypsin inhibitor activity
and tannins was negative and highly significant (r = -0.88, P < 0.001
), whereas between tannins and saponins it was significantly positive
(r = 0.96, P < 0.001).